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HRID 1616921생성일: 2026년 10월 24일

Hydrochloric Acid → 7-Methoxy-4a-methyl-3,4,4a,9a-tetrahydro[1]benzofuro[2,3-c]pyridine

https://huagongshe.com/ko/reaction/1616921

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium HydroxideHCID 14798—
반응물Lithium aluminum hydrideHCID 28112—
반응물7-methoxy-4a-methyl-3,4,4a,9a-tetrahydro-2Hbenzo[4,5]furo[2,3-c]pyridine-1-oneHCID 67323772—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물7-Methoxy-4a-methyl-3,4,4a,9a-tetrahydro[1]benzofuro[2,3-c]pyridineHCID 67324744—

반응 단계

To a solution of 7-methoxy-4a-methyl-3,4,4a,9a-tetrahydro-2Hbenzo[4,5]furo[2,3-c]pyridine-1-one (1.0 g, 4.30 mmol) in tetrahydrofuran (3 mL) was slowly added 1.0 M of lithium tetrahydroaluminate in tetrahydrofuran (2 mL). After 30 min stirring another portion of 1.0 M of lithium tetrahydroaluminate in tetrahydrofuran (1 mL) was added and the reaction was stirred for 2 h. The reaction was transferred into ice, 6N aqueous HCl was added followed by ethyl acetate. The aqueous layer was basified by adding NaOH and the product was extracted with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate, filtered and the solvent was evaporated to provide a colorless oil. The product was used in the next reaction step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08765779B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-b2c2e0662ec144ac90a842cebd40af0b
출처 메모uspto-grants-2014_07